US5104932A - Bituminous compositions containing residues of hydrolyzed or alcoholized polymers - Google Patents
Bituminous compositions containing residues of hydrolyzed or alcoholized polymers Download PDFInfo
- Publication number
- US5104932A US5104932A US07/658,626 US65862691A US5104932A US 5104932 A US5104932 A US 5104932A US 65862691 A US65862691 A US 65862691A US 5104932 A US5104932 A US 5104932A
- Authority
- US
- United States
- Prior art keywords
- mixtures
- bitumen
- asphalt
- hydrolysis
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 59
- 229920000642 polymer Polymers 0.000 title claims abstract description 38
- 239000010426 asphalt Substances 0.000 claims abstract description 46
- 239000002699 waste material Substances 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 22
- 238000006136 alcoholysis reaction Methods 0.000 claims abstract description 16
- 230000007062 hydrolysis Effects 0.000 claims abstract description 16
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 16
- 229920002635 polyurethane Polymers 0.000 claims abstract description 15
- 239000004814 polyurethane Substances 0.000 claims abstract description 15
- 229920000728 polyester Polymers 0.000 claims abstract description 14
- 239000003054 catalyst Substances 0.000 claims abstract description 7
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 7
- 150000001298 alcohols Chemical class 0.000 claims abstract description 6
- 150000001412 amines Chemical class 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims abstract description 5
- 239000011347 resin Substances 0.000 claims abstract description 5
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 4
- -1 alkali metal alkoxides Chemical class 0.000 claims description 8
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 8
- 239000011707 mineral Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 229920002732 Polyanhydride Polymers 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001414 amino alcohols Chemical class 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 229920000768 polyamine Polymers 0.000 claims description 2
- 238000006068 polycondensation reaction Methods 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 150000004679 hydroxides Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 239000000470 constituent Substances 0.000 abstract description 6
- 239000002253 acid Substances 0.000 abstract description 3
- 150000007513 acids Chemical class 0.000 abstract description 3
- 238000010348 incorporation Methods 0.000 abstract description 3
- 239000012948 isocyanate Substances 0.000 abstract description 3
- 150000002513 isocyanates Chemical class 0.000 abstract description 3
- 238000009833 condensation Methods 0.000 abstract description 2
- 230000005494 condensation Effects 0.000 abstract description 2
- 238000011065 in-situ storage Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 10
- 235000010755 mineral Nutrition 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000004064 recycling Methods 0.000 description 5
- 238000010276 construction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000013502 plastic waste Substances 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004634 thermosetting polymer Substances 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000010814 metallic waste Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229920006030 multiblock copolymer Polymers 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 238000005120 petroleum cracking Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- SYXYWTXQFUUWLP-UHFFFAOYSA-N sodium;butan-1-olate Chemical compound [Na+].CCCC[O-] SYXYWTXQFUUWLP-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
- C10C3/00—Working-up pitch, asphalt, bitumen
- C10C3/02—Working-up pitch, asphalt, bitumen by chemical means reaction
- C10C3/026—Working-up pitch, asphalt, bitumen by chemical means reaction with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
Definitions
- Polymers are at present used as additives in asphalts and bitumens used for roads or in industry, either for improving their workability by modifying the hot rheological properties, or for improving their physicochemical properties (cold brittleness, toughness, flexibility, stability, thermal susceptibility, mechanical strength with respect to shocks, vibrations, abrasions, etc.)
- the polymers used are thermoplastics (olefin copolymers or polymers), rubbers and in particular thermoplastic elastomers (multiblock copolymers of diolefins and styrene), or, to a lesser extent, thermosetting resins (polyurethanes, epoxy resin, phenol formaldehyde).
- these polymers can be used alone or in mixture.
- the mixtures of polymers essentially contain polyolefins, polyvinyl chloride, polystyrene and polyethylene terephthalate.
- the polymers are added in small quantities (generally 2 to 10% by weight) to bitumens, in the form of "simple” mixtures involving no chemical reaction or interaction between the constituents, or in the form of "complex” mixtures involving a chemical reaction or interaction between the polymer and certain constituents of the bitumen (asphaltenes, malthenes, resins, etc.), optionally in the presence of a third constituent (catalyst, reagent).
- bitumens in the form of "simple” mixtures involving no chemical reaction or interaction between the constituents, or in the form of “complex” mixtures involving a chemical reaction or interaction between the polymer and certain constituents of the bitumen (asphaltenes, malthenes, resins, etc.), optionally in the presence of a third constituent (catalyst, reagent).
- bitumens in the form of "simple” mixtures involving no chemical reaction or interaction between the constituents, or in the form of “complex
- the present invention relates to a simplified, economic process for the recycling of polymer waste in bitumens for roads or industry.
- This process is particularly suitable for the recycyling of "sterile car waste", i.e., plastic waste resulting from the breaking up of cars and which may possibly contain other polymer waste materials in small proportions, e.g., resulting from the breaking up of electric domestic appliances.
- sterile car waste i.e., plastic waste resulting from the breaking up of cars and which may possibly contain other polymer waste materials in small proportions, e.g., resulting from the breaking up of electric domestic appliances.
- sterile car waste or “car crushing waste” in fact designates all mineral and organic materials resulting from the crushing or cutting into pieces of in particular car bodies and to a lesser extent electric domestic appliances and industrial waste and obtained after the separation of the main metallic materials, e.g., by magnetic sorting processes, by gravitation or hydrocyclones, by flotation or performed manually.
- the recovered metallic materials are recycled as starting or raw materials for the metallurgical industry.
- bitumen (asphalte) used according to the present invention is a natural constituent of mineral and crude oils. It is obtained by deasphalting, e.g., by propane precipitation, or by the distillation of refining products (pitch) and/or petroleum cracking products. It can also be obtained from coal tar.
- bitumen fluxed e.g., with the aid of aromatic residues or distillates or an oxidized or blown bitumen.
- the fundamental originality of the present invention consists of efficientlyzing complex mixtures of organic polymers produced during the cutting into pieces and crushing of cars and to a lesser extent electric domestic appliances and industrial waste, while adding them to bituminous and asphalt binders and while improving certain properties with a view to their use in the coating of solid materials such as gravel, coatings or coverings and in particular in road construction, building, public works and special equipment.
- the mixture of sterile car waste or other equivalent polymer residues is, if necessary, washed with water to eliminate dirt. It then undergoes a hydrolysis and/or alcoholysis treatment, so as to transform at least a fraction of the polyurethanes of the sterile waste into alcohols, isocyanates or amines and/or a fraction of the polyesters of the sterile waste into acids and alcohols.
- the treatment consists of heating to a temperature generally between 80° and 200° C.
- the sterile car waste in the presence of 1 to 50% by weight of water, alcohols, aminoalcohols, amines or carboxylic acids, based on the weight of the sterile waste, optionally accompanied by the addition of a catalyst such as alkali metal hydroxide, soda or caustic potash, a salt or metal oxide, or an alkali metal alkoxide, e.g., at a concentration of 0.5 to 5% by weight based on the weight of the alcoholysis or hydrolysis reagent.
- Treatment is appropriately continued up to the hydrolysis and/or alcoholysis of at least 5 and preferably 20 to 90% by weight of the polyesters and/or polyurethanes contained in the polymer residues.
- bituminous mixture containing 1 to 80% by weight polymers.
- the mixture is kept for at least 5 minutes at a temperature between 120° and 230° C. It is also possible to add small quantities, e.g., 0.5 to 15% by weight based on the weight of the polymers of a catalyst such as a mineral or organic acid and/or a reagent such as a polyanhydride, polyacid, polyamine, polyalcohol or a polyisocyanate, so as to aid the in situ condensation of the acids, alcohols, amines or isocyanates formed during the pretreatment.
- a catalyst such as a mineral or organic acid
- a reagent such as a polyanhydride, polyacid, polyamine, polyalcohol or a polyisocyanate
- These compounds are able to react with one another or with certain constituents of the bitumen or asphalt.
- These polycondensation reagents and catalysts are known in the art and are preferably added to the bitumen or asphalt prior to the addition of the mixture of the pretreated polymers.
- thermoset resins into the bitumen. It is therefore very appropriate for adding to bitumens or asphalt, sterile car waste containing a fraction of polyurethane, polyester and/or polyepoxide resins, at a concentration which is generally between 4 and 15% by weight based on the weight of the organic sterile material.
- the polymer resins are reduced into powder form, the grains having an average size below 10 mm and preferably between 2 and 4 mm.
- a solvent such as halogenated or aromatic hydrocarbon during the hydrolysis and/or alcoholysis treatment of the sterile car waste.
- the solvent is then eliminated by distillation or evaporation prior to the addition of the bitumen.
- the concentrated mixture of sterile car waste obtained under the above conditions has a homogeneous appearance and rapidly dissolves during its dilution in excess of bitumen.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Road Paving Structures (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Description
Claims (12)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9002139 | 1990-02-21 | ||
| FR9002139A FR2658527B1 (en) | 1990-02-21 | 1990-02-21 | BITUMINOUS COMPOSITIONS CONTAINING RESIDUES OF HYDROLYSED OR ALCOHOLIC POLYMERS. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5104932A true US5104932A (en) | 1992-04-14 |
Family
ID=9393987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/658,626 Expired - Fee Related US5104932A (en) | 1990-02-21 | 1991-02-21 | Bituminous compositions containing residues of hydrolyzed or alcoholized polymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5104932A (en) |
| EP (1) | EP0443932B1 (en) |
| JP (1) | JPH04216868A (en) |
| CA (1) | CA2036576A1 (en) |
| DE (1) | DE69100599T2 (en) |
| FR (1) | FR2658527B1 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5308898A (en) * | 1990-02-21 | 1994-05-03 | Institut Francais Du Petrole | Bituminous compositions including residues of thermoplastic polymers with polyurethane foams and thermoset resin, etc. |
| US5635542A (en) * | 1994-06-23 | 1997-06-03 | Bayer Aktiengesellschaft | Process for the production of hydroxyl-group-containing compounds from polyurethane polyurea and/or polyurea wastes |
| US6015856A (en) * | 1995-11-10 | 2000-01-18 | Toyota Jidosha Kabushiki Kaisha | Composite resin material and method of forming the same |
| RU2527470C1 (en) * | 2013-03-22 | 2014-08-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Казанский государственный архитектурно-строительный университет" КГАСУ | Bitumen-urethane binder and method for production thereof |
| WO2024170558A1 (en) | 2023-02-14 | 2024-08-22 | Covestro Deutschland Ag | Method for cleaving urethanes |
| WO2025108308A1 (en) * | 2023-11-21 | 2025-05-30 | Basf Se | Composition obtained from depolymerization of polyurethane, process of preparing the same and bitumen composition comprising the same |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3311299B2 (en) * | 1998-10-21 | 2002-08-05 | 南己 伊藤 | Asphalt modifier and asphalt composition containing the same |
| JP4967885B2 (en) * | 1999-10-07 | 2012-07-04 | 日立化成工業株式会社 | Recycling method for cured epoxy resin |
| FR2944290B1 (en) * | 2009-04-09 | 2011-12-23 | Colas Sa | BITUMEN AND POLYMER ALLOYS - POLYMERIZATION IN BITUMEN MASS |
| JP7745443B2 (en) * | 2021-11-26 | 2025-09-29 | 花王株式会社 | Asphalt Modifier |
| JP2023110547A (en) * | 2022-01-28 | 2023-08-09 | 三菱ケミカル株式会社 | Method for treating cured thermosetting resin and method for producing thermoplastic resin |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4677146A (en) * | 1986-05-05 | 1987-06-30 | The Lubrizol Corporation | Modified asphalt compositions comprising a nitrogen derivative of an esterified copolymer |
| US4724245A (en) * | 1985-09-30 | 1988-02-09 | Screg Routes Et Travaux Publics | Process for the preparation of an aqueous emulsion composition of asphalt-polyurethane |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1522404A (en) * | 1967-03-14 | 1968-04-26 | Entpr Jean Lefebvre | Surfacing composition in particular for sports floors of evolution |
| NL7305619A (en) * | 1973-04-19 | 1974-10-22 |
-
1990
- 1990-02-21 FR FR9002139A patent/FR2658527B1/en not_active Expired - Lifetime
-
1991
- 1991-02-18 DE DE91400427T patent/DE69100599T2/en not_active Expired - Fee Related
- 1991-02-18 EP EP91400427A patent/EP0443932B1/en not_active Expired - Lifetime
- 1991-02-21 CA CA002036576A patent/CA2036576A1/en not_active Abandoned
- 1991-02-21 JP JP3027360A patent/JPH04216868A/en not_active Withdrawn
- 1991-02-21 US US07/658,626 patent/US5104932A/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4724245A (en) * | 1985-09-30 | 1988-02-09 | Screg Routes Et Travaux Publics | Process for the preparation of an aqueous emulsion composition of asphalt-polyurethane |
| US4677146A (en) * | 1986-05-05 | 1987-06-30 | The Lubrizol Corporation | Modified asphalt compositions comprising a nitrogen derivative of an esterified copolymer |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5308898A (en) * | 1990-02-21 | 1994-05-03 | Institut Francais Du Petrole | Bituminous compositions including residues of thermoplastic polymers with polyurethane foams and thermoset resin, etc. |
| US5635542A (en) * | 1994-06-23 | 1997-06-03 | Bayer Aktiengesellschaft | Process for the production of hydroxyl-group-containing compounds from polyurethane polyurea and/or polyurea wastes |
| US6015856A (en) * | 1995-11-10 | 2000-01-18 | Toyota Jidosha Kabushiki Kaisha | Composite resin material and method of forming the same |
| RU2527470C1 (en) * | 2013-03-22 | 2014-08-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Казанский государственный архитектурно-строительный университет" КГАСУ | Bitumen-urethane binder and method for production thereof |
| WO2024170558A1 (en) | 2023-02-14 | 2024-08-22 | Covestro Deutschland Ag | Method for cleaving urethanes |
| WO2025108308A1 (en) * | 2023-11-21 | 2025-05-30 | Basf Se | Composition obtained from depolymerization of polyurethane, process of preparing the same and bitumen composition comprising the same |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0443932A1 (en) | 1991-08-28 |
| DE69100599D1 (en) | 1993-12-16 |
| CA2036576A1 (en) | 1991-08-22 |
| JPH04216868A (en) | 1992-08-06 |
| FR2658527B1 (en) | 1992-05-15 |
| FR2658527A1 (en) | 1991-08-23 |
| EP0443932B1 (en) | 1993-11-10 |
| DE69100599T2 (en) | 1994-03-10 |
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